## Abstract Several strategies have been used to increase the biostability of medical‐grade polyurethanes while maintaining biocompatibility and mechanical properties. One approach is to chemically modify or replace the susceptible soft segment. Currently, poly(carbonate urethanes) (PCUs) are being
Oxidative mechanisms of poly(carbonate urethane) and poly(ether urethane) biodegradation:In vivo andin vitro correlations
✍ Scribed by Christenson, Elizabeth M. ;Anderson, James M. ;Hiltner, Anne
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 412 KB
- Volume
- 70A
- Category
- Article
- ISSN
- 0021-9304
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✦ Synopsis
Abstract
This study used an in vitro environment that simulated the microenvironment at the adherent cell‐material interface to reproduce and accelerate the biodegradation of poly(ether urethane) (PEU) and poly(carbonate urethane) (PCU). Polyurethane films were treated in vitro for 24 days in 20% hydrogen peroxide/0.1 M cobalt chloride solution at 37°C. Characterization with ATR‐FTIR and SEM showed soft segment and hard segment degradation consistent with the chemical changes observed after long‐term in vivo treatment. Overall, the PCU underwent less degradation and the degraded surface layer was much thinner than PEU. Nevertheless, the results supported a common oxidation mechanism for biodegradation of these polymers. The observed in vitro degradation was inhibited by adding an antioxidant to the polyurethane film. Our findings further support the use of the in vitro H~2~O~2~/CoCl~2~ system in evaluating the biostability of polyurethanes under accelerated conditions. © 2004 Wiley Periodicals, Inc. J Biomed Mater Res 70A: 245–255, 2004
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